Disease: Serum LDL cholesterol measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 5
rs1321655
ATP1A2
1 160124668 intron variant A/G;T snv 5
rs1456649
FMN2
1 240288305 intron variant G/C snv 3.0E-03 5
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99 6
rs4970834
CELSR2
0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 6
rs5176
LRP8
1 53246137 3 prime UTR variant T/G snv 6.4E-04 6
rs583104 1 109278685 downstream gene variant G/T snv 0.63 6
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 8
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
rs9436735
LEPR ; LEPROT
1 65419378 upstream gene variant C/G snv 2.5E-02 5
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 7
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 7
rs34183407
ALMS1
2 73454052 missense variant C/T snv 2.1E-05 3.5E-05 6
rs533617
APOB
2 21011100 missense variant T/C snv 3.1E-02 2.9E-02 6
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 7
rs11921179
TRH
3 129976195 intron variant G/A snv 0.96 5
rs16830551
GSK3B
3 119834031 intron variant C/T snv 2.4E-02 4
rs16860926 3 186609982 intron variant T/C snv 2.6E-02 4
rs17404153
DNAJC13
3 132444356 intron variant G/T snv 0.10 4